Hereditary choroidal dystrophy

DOID MESH PheWeb

H7_CHORDYSTROPTHY

No definition available.

Endpoint definition

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FinnGen phenotype data

321302 individuals

Apply sex-specific rule None

321302

Check conditions None

321302

Filter registries

Hospital Discharge: ICD-10 H31.2

Hospital discharge: ICD-9 3635

Hospital discharge: ICD-8 $!$

Cause of death: ICD-10 H31.2

Cause of death: ICD-9 3635

Cause of death: ICD-8 $!$

Check pre-conditions, main-only, mode, ICD version

Look only at ICD versions H.D: 10, 8, 9 ; C.O.D: 10, 8, 9

Check minimum number of events None

Include endpoints None

H7_CHORDYSTROPTHY

Extra metadata

Level in the ICD hierarchy 4

First used in FinnGen datafreeze DF2

Parent code in ICD-10 H31

Name in latin Dystrophia chorioideae hereditaria

Similar endpoints

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List of similar endpoints to Hereditary choroidal dystrophy based on the number of shared cases.

Broader endpoints:

Narrower endpoints:

None

Show all endpoint correlations

Summary Statistics

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Key figures

	All	Female	Male
Number of individuals	22	12	10
Unadjusted prevalence (%)	0.01	0.01	0.01
Mean age at first event (years)	50.76	42.40	60.78

Mortality

Follow-up	Absolute risk	HR [95% CI]	p	N
1998–2019	-	-	-	-
15 years	-	-	-	-
5 years	-	-	-	-
1 year	-	-	-	-

Age distribution of first events

Year distribution of first events

Cumulative Incidence

Correlations

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Index endpoint: H7_CHORDYSTROPTHY – Hereditary choroidal dystrophy
GWS hits:

Survival analyses between endpoints

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Plot

before Hereditary choroidal dystrophy
after Hereditary choroidal dystrophy

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Table

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Drugs most likely to be purchased after Hereditary choroidal dystrophy

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